marinobufagenin

chemical compound
ChemicalSubstance type_of_chemical_entity Q6764468
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marinobufagenin

Summary

marinobufagenin is a type of chemical entity[1]. marinobufagenin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (6 views/month).[2]

Key Facts

  • marinobufagenin's instance of is recorded as type of chemical entity[3].
  • marinobufagenin's chemical structure is recorded as Marinobufagin.svg[4].
  • marinobufagenin's CAS Registry Number is recorded as 470-42-8[5].
  • marinobufagenin's canonical SMILES is recorded as CC12CCC(CC1(CCC3C2CCC4(C35C(O5)CC4C6=COC(=O)C=C6)C)O)O[6].
  • marinobufagenin's InChI is recorded as InChI=1S/C24H32O5/c1-21-8-5-15(25)12-23(21,27)10-7-17-16(21)6-9-22(2)18(11-19-24(17,22)29-19)14-3-4-20(26)28-13-14/h3-4,13,15-19,25,27H,5-12H2,1-2H3/t15-,16-,17+,18+,19+,21+,22+,23-,24+/m0/s1[7].
  • marinobufagenin's InChIKey is recorded as JMNQTHQLNRILMH-OBBGIPBRSA-N[8].
  • marinobufagenin's chemical formula is recorded as C₂₄H₃₂O₅[9].
  • marinobufagenin's subclass of is recorded as bufanolide[10].
  • marinobufagenin's MeSH descriptor ID is recorded as C093896[11].
  • marinobufagenin's Freebase ID is recorded as /m/04q7z6k[12].
  • marinobufagenin's UNII is recorded as 3KBT25GV2B[13].
  • marinobufagenin's ChemSpider ID is recorded as 10142870[14].
  • marinobufagenin's PubChem CID is recorded as 11969465[15].
  • marinobufagenin's ChEBI ID is recorded as 146151[16].
  • marinobufagenin's found in taxon is recorded as Bufo[17].
  • marinobufagenin's found in taxon is recorded as Duttaphrynus melanostictus[18].
  • marinobufagenin's found in taxon is recorded as Bufo bankorensis[19].
  • marinobufagenin's found in taxon is recorded as Phrynoidis asper[20].
  • marinobufagenin's found in taxon is recorded as common toad[21].
  • marinobufagenin's found in taxon is recorded as Cane toad[22].
  • marinobufagenin's found in taxon is recorded as Berber toad[23].
  • marinobufagenin's isomeric SMILES is recorded as C[C@]12CCC@@HOC@@HO">[24].
  • marinobufagenin's LIPID MAPS ID is recorded as LMST01130078[25].
  • marinobufagenin's mass is recorded as {'unit': 'Q483261', 'amount': '+400.225'}[26].
  • marinobufagenin's NSC number is recorded as 234205[27].

Why It Matters

marinobufagenin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (6 views/month).[2] marinobufagenin has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[28]

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [3] . wikidata.org.
  2. [4] . wikidata.org.
  3. [5] . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] . PubChem. Retrieved . wikidata.org.
  5. [7] . PubChem. Retrieved . wikidata.org.
  6. [8] . PubChem. Retrieved . wikidata.org.
  7. [9] . PubChem. Retrieved . wikidata.org.
  8. [10] . wikidata.org.
  9. [11] . Medical Subject Headings. Retrieved . wikidata.org.
  10. [12] . wikidata.org.
  11. [13] . Global Substance Registration System. Retrieved . wikidata.org.
  12. [14] . Q2311683. Retrieved . wikidata.org.
  13. [15] . PubChem. Retrieved . wikidata.org.
  14. [16] . RCSB protein data bank. Retrieved . rcsb.org. Provenance: wikidata.org.
  15. [17] . Studies on toad venom (2): Examination of the drying processing method. wikidata.org.
  16. [18] . Chemical Constituents of Vietnamese Toad Venom, Collected From Bufo melanostictus Schneider. Part II. The Bufadienolides. wikidata.org.
  17. [19] . Occurrence of marinobufotoxin and telocinobufotoxin homologs in the skin of Bufo bankorensis BORBOUR.. wikidata.org.
  18. [20] . Studies on Steroids CCVIII. Bufadienolides from Bufo asper. wikidata.org.
  19. [21] . Isolation and characterization of cinobufagin 3-glutaroyl-L-arginine ester from Bufo bufo gargarizans Cantor.. wikidata.org.
  20. [22] . Digitalis-like Compounds of Toad Bile: Sulfation and Reduction of Bufadienolides Decrease Potency of Na+, K+- ATPase Inhibition. wikidata.org.
  21. [23] . Isolierung und Identifizierung der Steroide des Giftsekretes der Berberkröte (Pantherkröte)Bufo mauretanicus L. Über Krötengifte, 11. Mitteilung. wikidata.org.
  22. [24] . PubChem. Retrieved . wikidata.org.
  23. [25] . LIPID MAPS. Retrieved . lipidmaps.org. Provenance: wikidata.org.
  24. [26] . PubChem. Retrieved . wikidata.org.
  25. [27] . wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.org.
  2. [28] . Wikidata sitelinks. wikidata.org.

📑 Cite this page

Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). marinobufagenin. Retrieved May 3, 2026, from https://4ort.xyz/entity/marinobufagenin
MLA “marinobufagenin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/marinobufagenin.
BibTeX @misc{4ortxyz_marinobufagenin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{marinobufagenin}}, year = {2026}, url = {https://4ort.xyz/entity/marinobufagenin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): marinobufagenin — https://4ort.xyz/entity/marinobufagenin (retrieved 2026-05-03)

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